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(Received for publication, March 13, 1996, and in revised form, July 10, 1996)
From the Departments of The promoter activities of the genes for
cytochrome P450 2B1 (CYP2B1) and cytochrome P450 2C1
(CYP2C1) have been assayed by direct injection of
promoter-luciferase chimeric genes into rat liver. Activities of
minimal promoters for CYP2C1 and CYP2B1 were
detectable in untreated animals but were not increased by treatment of
the animals with phenobarbital. After insertion to the 5
Volume 271, Number 39,
Issue of September 27, 1996
pp. 23725-23728
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
,
§
Molecular and Integrative
Physiology and § Cell and Structural Biology, College of
Medicine at Urbana-Champaign, Urbana, Illinois 61801
side of the
minimal promoters of one to three copies of the CYP2B2
sequence from
2318 to
2155, a phenobarbital-responsive element in
primary hepatocyte cultures (Trottier, E., Belzil, A., Stoltz, C., and
Anderson, A. (1995) Gene (Amst.) 158, 263-268), phenobarbital treatment induced the activity of the
CYP2C1 promoter by 5-15-fold and the CYP2B1
promoter by 2.5-5-fold. Mutation of a basal transcription element-like
motif and a CCAAT/enhancer binding protein element in the
CYP2B1 proximal promoter region reduced expression, but
3-4-fold induction by phenobarbital was retained. Mutation of the
``Barbie box,'' a putative phenobarbital-responsive element (He,
J.-S., and Fulco, A. J. (1991) J. Biol. Chem. 266, 7864-7869) in the CYP2B1 proximal promoter did not reduce
the relative response to phenobarbital. These results demonstrate that
direct injection of DNA into rat liver may be used to assay
phenobarbital responsiveness of cytochrome P450 genes. In this system,
a distal CYP2B2 element mediates a response to
phenobarbital, and proximal elements, including the Barbie box, are not
required for the induction.
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